HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425366Generated: October 27, 2026
HCID 68430597, compound → HCID 59134307, compound
https://huagongshe.com/reaction/2425366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68430597 | HCID 68430597 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59134307 | HCID 59134307 | — |
Reaction Steps
To a solution of (3R*,4R*)-3-hydroxy-2,2,9-trimethyl-4-[(2-phenylethyl)amino]-3,4-dihydro-2H-pyrano[2,3-g]quinoline-7-carbonitrile described in Synthesis Example 14 (110 mg, 0.283 mmol) in acetic acid (5 mL), 10% Pd/C (22 mg) was added at room temperature, and the resulting mixture was stirred for 2 hours under hydrogen atmosphere. Upon the completion of the reaction, the resulting solution was filtered through celite, the solvent was distilled off and then sodium carbonate aqueous solution was added to the residue, and the resulting solution was extracted with chloroform, dried over anhydrous magnesium sulfate, and the solvent was distilled off to obtain crude product of (3R*,4S*)-7-aminomethyl-2,2,9-trimethyl-4-[(2-phenylethyl)amino]-3,4-dihydro-2H-pyrano[2,3-g]quinolin-3-ol (75.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964623B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-075d8f3459cc42a0a7848cf55aebd3cb |
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| Source note | uspto-grants-2011_06 |
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